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钆标记可生物降解的树突状-透明质酸杂化及其随后作为安全有效的磁共振成像造影剂的应用。

Gadolinium-Labeled Biodegradable Dendron-Hyaluronic Acid Hybrid and Its Subsequent Application as a Safe and Efficient Magnetic Resonance Imaging Contrast Agent.

机构信息

Huaxi MR Research Center (HMRRC), Department of Radiology, West China Hospital, Sichuan University , Chengdu, Sichuan 610041, China.

National Engineering Research Center for Biomaterials, Sichuan University , Chengdu 610064, China.

出版信息

ACS Appl Mater Interfaces. 2017 Jul 19;9(28):23508-23519. doi: 10.1021/acsami.7b06496. Epub 2017 Jul 10.

DOI:10.1021/acsami.7b06496
PMID:28656751
Abstract

Novel magnetic resonance imaging (MRI) contrast agents with high sensitivity and good biocompatibility are required for the diagnosis of cancer. Herein, we prepared and characterized the gadolinium [Gd(III)]-labeled peptide dendron-hyaluronic acid (HA) conjugate-based hybrid (dendronized-HA-DOTA-Gd) by combining the advantages of HA and the peptide dendron. The dendronized-HA-DOTA-Gd hybrid with 3.8% Gd(III) as weight percentage showed a negative zeta potential (-35 mV). The in vitro degradation results indicated that the dendronized-HA-DOTA-Gd hybrid degraded into products with low molecular weights in the presence of hyaluronidase. The dendronized-HA-DOTA-Gd hybrid showed a 3-fold increase in longitudinal relaxivity and much higher in vivo signal enhancement in 4T1 breast tumors of mice compared with clinical Magnevist (Gd-DTPA). The dendronized-HA-DOTA-Gd hybrid had a higher accumulation in tumors than Gd-DTPA; it was 2-3-fold after administration. Meanwhile, the polymeric hybrid resulted in low Gd(III) residue in the body compared with that of Gd-DTPA. The systematic biosafety evaluations, including blood compatibility and toxicity assessments, suggested that the dendronized-HA-DOTA-Gd hybrid exhibited good biocompatibility. Thus, the gadolinium-labeled and dendronized HA hybrid shows promise as a safe and efficient macromolecular MRI contrast agent based on high sensitivity, low residue content in the body, and good biosafety.

摘要

新型磁共振成像(MRI)对比剂需要具有高灵敏度和良好的生物相容性,以便用于癌症的诊断。在此,我们通过结合透明质酸(HA)和肽树枝状大分子的优势,制备并表征了基于钆[Gd(III)]标记的肽树枝状大分子-透明质酸(HA)偶联物的杂化体(树枝状大分子化-HA-DOTA-Gd)。树枝状大分子化-HA-DOTA-Gd 杂化物的重量百分比为 3.8%的 Gd(III),其具有负的 Zeta 电位(-35 mV)。体外降解结果表明,树枝状大分子化-HA-DOTA-Gd 杂化物在透明质酸酶存在的情况下降解为低分子量产物。与临床用 Magnevist(Gd-DTPA)相比,树枝状大分子化-HA-DOTA-Gd 杂化物的纵向弛豫率提高了 3 倍,在 4T1 乳腺癌小鼠的体内信号增强也更高。与 Gd-DTPA 相比,树枝状大分子化-HA-DOTA-Gd 杂化物在肿瘤中的积累更高;给药后是其 2-3 倍。同时,与 Gd-DTPA 相比,聚合物杂化物在体内导致的 Gd(III)残留量较低。包括血液相容性和毒性评估在内的系统生物安全性评价表明,树枝状大分子化-HA-DOTA-Gd 杂化物具有良好的生物相容性。因此,基于高灵敏度、体内残留量低和良好的生物安全性,标记了 Gd 的树枝状大分子化 HA 杂化物具有作为安全有效的大分子 MRI 对比剂的潜力。

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